view | regionname | pos | ref | alt | annotation | impact | samples | ahapids | achapids | acthapids | actghapids | ac | an | af | len | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length
|
cds cds pos length
|
aa aa pos length
|
distance | status | chr | external |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
PLXNB1_chr3_48398854_48435086 | 48400315 | TGCTCAGG others(55): Show |
T | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(179): Show |
a0001a0002a0005others(9): Show | a0001c0001a0001c0003a0001c0006others(21): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(24): Show | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(66): Show | 182 | 318 | 0.5723 | -62 | c.*41 others(73): Show |
PLXNB1 | ENSG00000164050.13 | transcript | ENST00000296440.11 | protein_coding | 3538 | chr3 | TogoVar | |||||||
PLXNC1_chr12_94143577_94312675 | 94177149 | GTATATAT others(55): Show |
G | intron_variant | MODIFIER | HG00621.hp2 HG00673.hp1 HG02015.hp1 others(6): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0016others(4): Show | a0001c0001t0001g0028a0001c0001t0003g0047a0001c0001t0016g0196others(6): Show | 9 | 298 | 0.0302 | -62 | c.120 others(81): Show |
PLXNC1 | ENSG00000136040.9 | transcript | ENST00000258526.9 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
PLXNC1_chr12_94143577_94312675 | 94177157 | ATATGTAT others(55): Show |
A | intron_variant | MODIFIER | HG02630.hp1 HG03579.hp1 |
a0001 | a0001c0001a0001c0007 | a0001c0001t0001a0001c0007t0003 | a0001c0001t0001g0154a0001c0007t0003g0197 | 2 | 298 | 0.0067 | -62 | c.120 others(81): Show |
PLXNC1 | ENSG00000136040.9 | transcript | ENST00000258526.9 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
POLG_chr15_89311320_89339824 | 89325049 | TGAGTGAG others(55): Show |
T | intron_variant | MODIFIER | HG03225.hp2 NA18747.hp2 |
a0001 | a0001c0001a0001c0009 | a0001c0001t0001a0001c0009t0001 | a0001c0001t0001g0079a0001c0009t0001g0205 | 2 | 398 | 0.0050 | -62 | c.194 others(79): Show |
POLG | ENSG00000140521.18 | transcript | ENST00000268124.11 | protein_coding | 10/22 | chr15 | TogoVar | |||||||
POLRMT_chr19_612221_638537 | 620925 | GGGGCGCC others(55): Show |
G | intron_variant | MODIFIER | HG00408.hp1 HG00423.hp2 HG00621.hp1 others(64): Show |
a0002a0003a0004others(8): Show | a0002c0006a0002c0044a0002c0048others(12): Show | a0002c0006t0001a0002c0006t0002a0002c0044t0002others(16): Show | a0002c0006t0001g0050a0002c0006t0002g0026a0002c0006t0002g0251others(54): Show | 67 | 422 | 0.1588 | -62 | c.264 others(78): Show |
POLRMT | ENSG00000099821.14 | transcript | ENST00000588649.7 | protein_coding | 10/20 | chr19 | TogoVar | |||||||
POTEJ_chr2_130606440_130663037 | 130613266 | ATATATAT others(55): Show |
A | intron_variant | MODIFIER | NA18952.hp2 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0024 | 1 | 131 | 0.0076 | -62 | c.410 others(79): Show |
POTEJ | ENSG00000222038.4 | transcript | ENST00000409602.2 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
POTEM_chr14_18962434_19008752 | 18969280 | TATACACA others(55): Show |
T | intron_variant | MODIFIER | HG01243.hp2 | a0010 | a0010c0014 | a0010c0014t0013 | a0010c0014t0013g0066 | 1 | 67 | 0.0149 | -62 | c.521 others(79): Show |
POTEM | ENSG00000222036.8 | transcript | ENST00000547889.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
POU6F2_chr7_38972909_39473601 | 39419085 | GTATATGT others(55): Show |
G | intron_variant | MODIFIER | HG02976.hp1 HG03486.hp1 |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0089a0001c0002t0001g0090 | 2 | 170 | 0.0118 | -62 | c.111 others(83): Show |
POU6F2 | ENSG00000106536.21 | transcript | ENST00000518318.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
PPCDC_chr15_75018590_75055726 | 75024964 | CCCAGGCT others(55): Show |
C | intron_variant | MODIFIER | NA18974.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0169 | 1 | 398 | 0.0025 | -62 | c.-73 others(79): Show |
PPCDC | ENSG00000138621.12 | transcript | ENST00000342932.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
PPP1R9A_chr7_94902594_95301400 | 95181747 | GTCACATA others(55): Show |
G | intron_variant | MODIFIER | HG02615.hp1 HG03098.hp1 HG03130.hp2 |
a0001a0015 | a0001c0002a0015c0024 | a0001c0002t0003a0015c0024t0003 | a0001c0002t0003g0111a0001c0002t0003g0199a0015c0024t0003g0202 | 3 | 290 | 0.0103 | -62 | c.175 others(83): Show |
PPP1R9A | ENSG00000158528.12 | transcript | ENST00000433360.6 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
PPP2R2D_chr10_131896008_131964834 | 131917618 | CACAGTGT others(55): Show |
C | intron_variant | MODIFIER | NA21309.hp2 | a0001 | a0001c0001 | a0001c0001t0081 | a0001c0001t0081g0258 | 1 | 394 | 0.0025 | -62 | c.100 others(81): Show |
PPP2R2D | ENSG00000175470.20 | transcript | ENST00000455566.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | ||||||
PPP2R2D_chr10_131896008_131964834 | 131919055 | TAGGGACC others(55): Show |
T | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(117): Show |
a0001a0003 | a0001c0001a0001c0003a0001c0005others(1): Show | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(50): Show | a0001c0001t0003g0037a0001c0001t0003g0074a0001c0001t0003g0075others(109): Show | 120 | 394 | 0.3046 | -62 | c.101 others(81): Show |
PPP2R2D | ENSG00000175470.20 | transcript | ENST00000455566.6 | protein_coding | 2/8 | chr10 | TogoVar | |||||||
PPP2R5C_chr14_101756709_101932977 | 101782353 | CTCTCTCT others(55): Show |
C | intron_variant | MODIFIER | HG02451.hp1 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0092 | 1 | 138 | 0.0073 | -62 | c.94- others(77): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | TogoVar | |||||||
PPP4R3A_chr14_91452508_91515310 | 91507358 | GTATATAT others(55): Show |
G | intron_variant | MODIFIER | HG01515.hp2 HG01517.hp1 |
a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0353a0001c0003t0001g0354 | 2 | 370 | 0.0054 | -62 | c.142 others(79): Show |
PPP4R3A | ENSG00000100796.18 | transcript | ENST00000554943.6 | protein_coding | 1/14 | chr14 | TogoVar | |||||||
PPP5C_chr19_46342087_46395975 | 46389362 | AACACACA others(55): Show |
A | intron_variant | MODIFIER | HG01070.hp1 HG01071.hp2 HG01243.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0007 | a0001c0001t0001g0133a0001c0001t0001g0195a0001c0001t0001g0198others(1): Show | 4 | 394 | 0.0102 | -62 | c.135 others(79): Show |
PPP5C | ENSG00000011485.15 | transcript | ENST00000012443.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
PPP6R2_chr22_50338327_50450090 | 50344807 | CCCCCCCC others(55): Show |
C | intron_variant | MODIFIER | HG02074.hp1 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0202 | 1 | 340 | 0.0029 | -62 | c.-14 others(81): Show |
PPP6R2 | ENSG00000100239.16 | transcript | ENST00000612753.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
PPP6R2_chr22_50338327_50450090 | 50433264 | TCTGGAGG others(55): Show |
T | intron_variant | MODIFIER | HG02572.hp2 HG03041.hp2 |
a0009 | a0009c0016 | a0009c0016t0008 | a0009c0016t0008g0221a0009c0016t0008g0222 | 2 | 340 | 0.0059 | -62 | c.140 others(80): Show |
PPP6R2 | ENSG00000100239.16 | transcript | ENST00000612753.5 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
PPP6R2_chr22_50338327_50450090 | 50433383 | TTTGCTCT others(55): Show |
T | intron_variant | MODIFIER | HG02165.hp1 HG03471.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0074a0001c0001t0001g0295 | 2 | 340 | 0.0059 | -62 | c.140 others(81): Show |
PPP6R2 | ENSG00000100239.16 | transcript | ENST00000612753.5 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
PPP6R2_chr22_50338327_50450090 | 50433549 | CGCTGGGC others(55): Show |
C | intron_variant | MODIFIER | HG02723.hp1 | a0001 | a0001c0002 | a0001c0002t0004 | a0001c0002t0004g0332 | 1 | 340 | 0.0029 | -62 | c.140 others(81): Show |
PPP6R2 | ENSG00000100239.16 | transcript | ENST00000612753.5 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
PPP6R2_chr22_50338327_50450090 | 50433698 | TCTGGAGG others(55): Show |
T | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(141): Show |
a0001a0005a0006others(5): Show | a0001c0001a0001c0003a0001c0005others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(27): Show | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0223others(141): Show | 144 | 340 | 0.4235 | -62 | c.140 others(81): Show |
PPP6R2 | ENSG00000100239.16 | transcript | ENST00000612753.5 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
PPP6R2_chr22_50338327_50450090 | 50433916 | GCAGACGC others(55): Show |
G | intron_variant | MODIFIER | HG03471.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0295 | 1 | 340 | 0.0029 | -62 | c.140 others(80): Show |
PPP6R2 | ENSG00000100239.16 | transcript | ENST00000612753.5 | protein_coding | 12/23 | chr22 | TogoVar | |||||||
PPP6R2_chr22_50338327_50450090 | 50434157 | CGGGGGCG others(55): Show |
C | intron_variant | MODIFIER | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(14): Show |
a0001a0009a0020 | a0001c0001a0001c0003a0001c0008others(3): Show | a0001c0001t0001a0001c0001t0029a0001c0003t0002others(4): Show | a0001c0001t0001g0255a0001c0001t0029g0238a0001c0003t0002g0180others(14): Show | 17 | 340 | 0.0500 | -62 | c.140 others(79): Show |
PPP6R2 | ENSG00000100239.16 | transcript | ENST00000612753.5 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
PPWD1_chr5_65558296_65592549 | 65578723 | CATATATA others(55): Show |
C | intron_variant | MODIFIER | HG01884.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0170 | 1 | 384 | 0.0026 | -62 | c.116 others(79): Show |
PPWD1 | ENSG00000113593.12 | transcript | ENST00000261308.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
PRDM15_chr21_41793225_41884344 | 41856199 | TCCTTTCC others(55): Show |
T | intron_variant | MODIFIER | NA18954.hp1 | a0001 | a0001c0001 | a0001c0001t0009 | a0001c0001t0009g0215 | 1 | 406 | 0.0025 | -62 | c.285 others(77): Show |
PRDM15 | ENSG00000141956.14 | transcript | ENST00000398548.6 | protein_coding | 4/23 | chr21 | TogoVar | |||||||
PRDM6_chr5_123084241_123199266 | 123112133 | AGCTCCTA others(55): Show |
A | intron_variant | MODIFIER | HG03209.hp1 | a0004 | a0004c0004 | a0004c0004t0072 | a0004c0004t0072g0230 | 1 | 312 | 0.0032 | -62 | c.900 others(81): Show |
PRDM6 | ENSG00000061455.11 | transcript | ENST00000407847.5 | protein_coding | 3/7 | chr5 | TogoVar | |||||||
PRKCZ_chr1_2045411_2190395 | 2121824 | AGGGTCGT others(55): Show |
A | intron_variant | MODIFIER | HG02572.hp1 HG02735.hp1 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0001 | a0001c0001t0001g0242a0001c0003t0001g0137 | 2 | 286 | 0.0070 | -62 | c.335 others(81): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2122303 | GGTGGTAG others(55): Show |
G | intron_variant | MODIFIER | HG01109.hp1 HG02683.hp2 NA18964.hp2 others(2): Show |
a0001 | a0001c0002a0001c0003 | a0001c0002t0001a0001c0003t0001a0001c0003t0003 | a0001c0002t0001g0070a0001c0002t0001g0208a0001c0002t0001g0209others(2): Show | 5 | 286 | 0.0175 | -62 | c.335 others(81): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2122309 | AGGGTCGT others(55): Show |
A | intron_variant | MODIFIER | HG02165.hp1 HG03139.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0008 | a0001c0001t0001g0251a0001c0001t0008g0241 | 2 | 286 | 0.0070 | -62 | c.335 others(81): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2122368 | GGTGGTTA others(55): Show |
G | intron_variant | MODIFIER | HG02572.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0242 | 1 | 286 | 0.0035 | -62 | c.335 others(81): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2122417 | ACGGTGGT others(55): Show |
A | intron_variant | MODIFIER | HG02165.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0251 | 1 | 286 | 0.0035 | -62 | c.335 others(81): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | chr1 | TogoVar | |||||||
PRKCZ_chr1_2045411_2190395 | 2122419 | GGTGGTAG others(55): Show |
G | intron_variant | MODIFIER | HG01123.hp2 HG01192.hp2 HG02055.hp1 others(1): Show |
a0001 | a0001c0002a0001c0003 | a0001c0002t0001a0001c0003t0003a0001c0003t0004 | a0001c0002t0001g0221a0001c0003t0003g0193a0001c0003t0003g0199others(1): Show | 4 | 286 | 0.0140 | -62 | c.335 others(81): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2122425 | AGGGTCGT others(55): Show |
A | intron_variant | MODIFIER | HG02723.hp2 HG02809.hp2 HG02965.hp1 others(5): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0004t0001 | a0001c0001t0001g0048a0001c0001t0001g0105a0001c0001t0001g0106others(5): Show | 8 | 286 | 0.0280 | -62 | c.335 others(81): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2122985 | GGTGGTAG others(55): Show |
G | intron_variant | MODIFIER | HG02622.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0113 | 1 | 286 | 0.0035 | -62 | c.335 others(81): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2122991 | AGGGTCGT others(55): Show |
A | intron_variant | MODIFIER | HG01109.hp2 HG02155.hp2 HG02572.hp2 others(1): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0004t0001a0001c0004t0002 | a0001c0001t0001g0121a0001c0001t0001g0174a0001c0004t0001g0145others(1): Show | 4 | 286 | 0.0140 | -62 | c.335 others(81): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2123206 | CACGGTGG others(55): Show |
C | intron_variant | MODIFIER | HG00642.hp1 HG01192.hp2 HG02027.hp1 others(10): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0002t0001a0001c0002t0004others(2): Show | a0001c0001t0001g0066a0001c0002t0001g0167a0001c0002t0001g0207others(10): Show | 13 | 286 | 0.0455 | -62 | c.335 others(81): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | chr1 | TogoVar | |||||||
PRKCZ_chr1_2045411_2190395 | 2123209 | GGTGGTAG others(55): Show |
G | intron_variant | MODIFIER | HG01099.hp1 | a0001 | a0001c0001 | a0001c0001t0015 | a0001c0001t0015g0014 | 1 | 286 | 0.0035 | -62 | c.335 others(81): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2123215 | AGGGTCGT others(55): Show |
A | intron_variant | MODIFIER | NA18942.hp1 NA18948.hp2 NA19011.hp1 others(1): Show |
a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0008a0001c0004t0001g0009a0001c0004t0001g0011others(1): Show | 4 | 286 | 0.0140 | -62 | c.335 others(81): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PRKG1_chr10_51069487_52303350 | 51553890 | TAATATAT others(55): Show |
T | intron_variant | MODIFIER | HG03453.hp1 | a0001 | a0001c0001 | a0001c0001t0015 | a0001c0001t0015g0010 | 1 | 64 | 0.0156 | -62 | c.592 others(81): Show |
PRKG1 | ENSG00000185532.20 | transcript | ENST00000373980.11 | protein_coding | 3/17 | chr10 | TogoVar | |||||||
PRODH_chr22_18907781_18941293 | 18908260 | TTGAATTC others(55): Show |
T | downstream_gene_variant | MODIFIER | NA19075.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0013 | 1 | 409 | 0.0024 | -62 | c.*48 others(73): Show |
PRODH | ENSG00000100033.17 | transcript | ENST00000357068.11 | protein_coding | 4520 | chr22 | TogoVar | |||||||
PSTPIP2_chr18_45978536_46077260 | 46076254 | ATTTTTGC others(55): Show |
A | upstream_gene_variant | MODIFIER | NA19065.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0030 | 1 | 316 | 0.0032 | -62 | c.-41 others(73): Show |
PSTPIP2 | ENSG00000152229.18 | transcript | ENST00000409746.5 | protein_coding | 3995 | chr18 | TogoVar | |||||||
PTGFR_chr1_78485974_78545701 | 78532410 | ATATATAT others(55): Show |
A | intron_variant | MODIFIER | HG00140.hp2 HG00558.hp2 HG00642.hp1 others(31): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(5): Show | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0027others(23): Show | 34 | 386 | 0.0881 | -62 | c.799 others(79): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PTP4A2_chr1_31901421_31943368 | 31908113 | AATATATA others(55): Show |
A | 3_prime_UTR_variant | MODIFIER | HG00544.hp2 HG01081.hp1 NA19068.hp2 |
a0001 | a0001c0001 | a0001c0001t0048a0001c0001t0152 | a0001c0001t0048g0175a0001c0001t0048g0218a0001c0001t0152g0196 | 3 | 354 | 0.0085 | -62 | c.*67 others(71): Show |
PTP4A2 | ENSG00000184007.22 | transcript | ENST00000647444.2 | protein_coding | 6/6 | 677 | chr1 | TogoVar | ||||||
PTPN5_chr11_18722928_18796798 | 18793954 | CACTGATT others(55): Show |
C | upstream_gene_variant | MODIFIER | NA18968.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0247 | 1 | 388 | 0.0026 | -62 | c.-26 others(73): Show |
PTPN5 | ENSG00000110786.18 | transcript | ENST00000358540.7 | protein_coding | 2157 | chr11 | TogoVar | |||||||
PVR_chr19_44638910_44671162 | 44645121 | ATATTATA others(55): Show |
A | intron_variant | MODIFIER | NA18950.hp1 NA18993.hp2 |
a0002a0010 | a0002c0002a0010c0008 | a0002c0002t0003a0010c0008t0004 | a0002c0002t0003g0042a0010c0008t0004g0042 | 2 | 412 | 0.0049 | -62 | c.79+ others(76): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
PVR_chr19_44638910_44671162 | 44668287 | TTATATTT others(55): Show |
T | downstream_gene_variant | MODIFIER | HG02451.hp1 NA20300.hp1 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0046a0002c0002t0085 | a0001c0001t0046g0095a0002c0002t0085g0064 | 2 | 412 | 0.0049 | -62 | c.*64 others(73): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2126 | chr19 | TogoVar | |||||||
PXDN_chr2_1626887_1749515 | 1710857 | TCCACCAG others(55): Show |
T | intron_variant | MODIFIER | HG02523.hp1 HG03492.hp2 NA18997.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0003 | a0001c0001t0001g0070a0001c0001t0001g0214a0001c0002t0003g0112others(1): Show | 4 | 322 | 0.0124 | -62 | c.201 others(81): Show |
PXDN | ENSG00000130508.11 | transcript | ENST00000252804.9 | protein_coding | 1/22 | chr2 | TogoVar | |||||||
PXK_chr3_58327892_58431127 | 58334956 | TGTCTGTG others(55): Show |
T | intron_variant | MODIFIER | HG03540.hp1 | a0003 | a0003c0003 | a0003c0003t0002 | a0003c0003t0002g0053 | 1 | 300 | 0.0033 | -62 | c.102 others(79): Show |
PXK | ENSG00000168297.16 | transcript | ENST00000356151.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
PXYLP1_chr3_141226825_141299924 | 141248634 | TACACACG others(55): Show |
T | intron_variant | MODIFIER | HG01515.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0111 | 1 | 384 | 0.0026 | -62 | c.-53 others(81): Show |
PXYLP1 | ENSG00000155893.13 | transcript | ENST00000286353.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
PZP_chr12_9143840_9213395 | 9197777 | CATAATAT others(55): Show |
C | intron_variant | MODIFIER | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(84): Show |
a0002a0005a0014others(9): Show | a0002c0002a0005c0008a0005c0019others(11): Show | a0002c0002t0001a0005c0008t0001a0005c0019t0001others(11): Show | a0002c0002t0001g0003a0002c0002t0001g0010a0002c0002t0001g0046others(75): Show | 87 | 334 | 0.2605 | -62 | c.756 others(77): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | TogoVar | |||||||
RAB11FIP3_chr16_420649_528011 | 482134 | GCAGGCAG others(55): Show |
G | intron_variant | MODIFIER | HG01261.hp2 | a0001 | a0001c0002 | a0001c0002t0009 | a0001c0002t0009g0254 | 1 | 295 | 0.0034 | -62 | c.904 others(77): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | TogoVar |